Efficient site management is essential for an effective trial and rapid collection of accurate results.

Our CRAs are highly-trained and available 24/7. They are adept at building long-term partnerships with investigators and supporting efficient trial recruitment, as well as ensuring proper data quality and consistency.

Throughout the study, our team provides support in areas, including:

  • site personnel training and education
  • study drug and non-drug supplies logistics
  • tracking regulatory document revisions
  • tracking protocol deviations
  • tracking subject status within the trial